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Completed Phase 4 Interventional

A Study Evaluating the Efficacy and Safety of Adding Symlin® to Lantus® (Insulin Glargine) in Subjects With Type 2 Diabetes

ClinicalTrials.gov ID: NCT00240253

Public ClinicalTrials.gov record NCT00240253. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 5:07 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study Evaluating the Efficacy and Safety of Adding Symlin® to Lantus® (Insulin Glargine) in Subjects With Type 2 Diabetes Who Are Not Achieving Glycemic Targets

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the efficacy and safety of adding Symlin to an established regimen of insulin glargine in subjects with type 2 diabetes who are not achieving glycemic targets.

Study identification

NCT ID
NCT00240253
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
AstraZeneca
Industry
Enrollment
200 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2005 (Type not available)
Primary completion
Jun 2006 (Actual)
Completion
Jun 2006 (Actual)
Last update posted
Mar 31, 2015

2005 – 2006

United States locations

U.S. sites
34
U.S. states
24
U.S. cities
34
Facility City State ZIP Site status
Research Site Phoenix Arizona — —
Research Site Concord California — —
Research Site La Jolla California — —
Research Site Los Gatos California — —
Research Site Salinas California — —
Research Site Walnut Creek California — —
Research Site Denver Colorado — —
Research Site New Britain Connecticut — —
Research Site Washington D.C. District of Columbia — —
Research Site Palm Harbor Florida — —
Research Site Atlanta Georgia — —
Research Site Indianapolis Indiana — —
Research Site Wichita Kansas — —
Research Site Lexington Kentucky — —
Research Site Baton Rouge Louisiana — —
Research Site Bloomfield Hills Michigan — —
Research Site Detroit Michigan — —
Research Site Grand Rapids Michigan — —
Research Site Chesterfield Missouri — —
Research Site Butte Montana — —
Research Site Omaha Nebraska — —
Research Site Charlotte North Carolina — —
Research Site Durham North Carolina — —
Research Site Cincinnati Ohio — —
Research Site Oklahoma City Oklahoma — —
Research Site Medford Oregon — —
Research Site Portland Oregon — —
Research Site Philadelphia Pennsylvania — —
Research Site Tipton Pennsylvania — —
Research Site Nashville Tennessee — —
Research Site Dallas Texas — —
Research Site Charlottesville Virginia — —
Research Site Olympia Washington — —
Research Site Spokane Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00240253, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 31, 2015 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00240253 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →